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Induction Agents
Each agent has its own mode of action
All result in loss of consciousness
Unconsciousness is achieved once sufficient brain levels obtained
Movement of agent from blood to brain occurs via concentration gradients
Speed of induction and recovery determined by the lipid solubility of agent
Drugs that are highly lipid soluble cross cell membranes faster (faster onset and recovery)
Upon injection of induction agent
Upon injection of agent
High levels of drug in blood
These drugs rapidly are taken up by brain
Low level in muscle, fat, and organs
Once injection is completed
Levels in blood drop
Agent leaves brain because of concentration gradient
Agent leaves blood and enters tissues
Recovery occurs
Once levels in brain become low enough, the animal recovers consciousness
The drug however is still in the fat, muscle, and tissues
Different drugs excreted differently, but patient not fully recovered until all agent has left body (may take >24 hrs)
Propofol
Ultra-short acting
Nonbarbiturate
Used for induction and maintenance of anesthesia
Also used for treatment of status epilepticus
Non-Controlled — but many practices will still record in drug log as a precaution
Pharmacology
Minimal water solubility
Milky, but can be given IV
Onset of action: 30-60 sec Duration: 5-10 min
Propofol effects
Major effects
Dose dependent CNS depression
Cardiac depression — bradycardia, decreased CO, hypotension
Respiratory depressant — APNEA
Twitching during induction
Muscle relaxation
Minor effects
Relatively safe for animals with liver and kidney dysfunction
Appetite stimulant at low doses
Antiemetic
Decreases intracranial and intraocular pressure
Adverse effects
Excitement during induction if injection is too slow
Hypotension — may be prolonged if patient previously hypotensive
Induction apnea
Irritating when given SQ
Heinz body formation in repeated dosing to cats
Use
Give dose slowly to effect (bolus first half, then give to effect)
Can also be used as CRI to maintain GA
Manufacturer recommends discarding product after 6 hrs of opening
Cost is 4X that of ket/val
Etomidate
Duration of action: 3-5 min
Effects
Minimal effects on cardio and resp systems
Little analgesia
Anticonvulsant
Good muscle relaxation
Pain on injection
Nausea & vomiting
Not available in Canada
Alfaxalone
Ultrashort-acting injectable anesthetic
Wide margin of safety
Relatively new in Canada
Can be given IV or IM
Works similar to propofol
Effects
Dose-dependent CNS depression & resp depression
Apnea
Hypotension (especially when used with inhalant)
Muscle relaxation
No analgesia
Cardio system depression minimal
Smooth induction, no excitement
Not irritating if inadvertently given perivascular
Use
Given similar to propofol — bolus ~half, then to effect
Duration 5-10 min
Repeated dose does not prolong recovery, therefore CRIs are possible
Better shelf life
Dissociative Anesthetics
Drugs
Ketamine
Ketamine-Diazepam combo
Onset of action
1-2 min IV
10 min IM
Duration
20-30 min
Higher dose increases duration, not depth
Use
Can be given IM or IV
Dissociative Anesthetics effects
Effects
Cataleptic state — patient does not respond to stimulus and maintains muscle rigidity
Intact reflexes — difficult to assess depth
Central eye that has mydriatic pupils and open lids
Normal or increased muscle tone
Analgesia to skin and limbs, limited to viscera
Amnesia — humans
Increased sensory stimuli
Do not become bradycardic
Adverse effects
Stimulation to sound, light, etc.
Abnormal behaviors in recovery
Nystagmus
Decrease contractility — patient with heart disease cannot compensate
Predispose to development of arrhythmias
Increase salivation and resp secretions
Tissue irritation if given perivascular
Increased intracranial and intraocular pressure
Ketamine
IM use is limited to fractious cats
Can be given orally to fractious cats
If given repeated doses, can increase risk of seizure activity and prolong recovery
Undergoes hepatic metabolism and renal excretion — use caution if renal or hepatic disease
Ketamine-Diazepam
IV induction for cats and dogs
Equal volumes of each mixed in same syringe (watch for precipitation)
Give to effect
Duration: 5-10 min
Minimal cardiac depression
Good muscle relaxation
Superior recovery
Some analgesia
Guaifenesin (GGE)
Not an anesthetic on its own — given in combination with other agents
Needs to be reconstituted
Effects
Muscle relaxation
Minimal cardiopulmonary effects
Adverse effects
Can cause thrombophlebitis or tissue reaction if given perivascular
Use
Used in combination with other agents for induction and maintenance of anesthesia
Given rapidly IV after premed until signs of knuckling noticed, then induction agent given